The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125602351 12560235 1 I 20130821 0 20160714 20160714 DIR 60.55 YR M N 69.50000 KG 20160713 N MD US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125602351 12560235 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1470 MG
125602351 12560235 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 80 MG
125602351 12560235 3 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 400 MG
125602351 12560235 4 SS PREDNISONE. PREDNISONE 1 0 1000 MG
125602351 12560235 5 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 3.2 MG
125602351 12560235 6 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 700 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125602351 12560235 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125602351 12560235 Abdominal pain
125602351 12560235 Nausea
125602351 12560235 Pseudomonas infection
125602351 12560235 Staphylococcal infection
125602351 12560235 Wound

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125602351 12560235 1 20130804 0
125602351 12560235 2 20130803 0
125602351 12560235 3 20130803 0
125602351 12560235 4 20130805 0
125602351 12560235 5 20130803 0
125602351 12560235 6 20130803 0